AU2017322733B2 - Genome edited primary B cell and methods of making and using - Google Patents

Genome edited primary B cell and methods of making and using Download PDF

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AU2017322733B2
AU2017322733B2 AU2017322733A AU2017322733A AU2017322733B2 AU 2017322733 B2 AU2017322733 B2 AU 2017322733B2 AU 2017322733 A AU2017322733 A AU 2017322733A AU 2017322733 A AU2017322733 A AU 2017322733A AU 2017322733 B2 AU2017322733 B2 AU 2017322733B2
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cell
primary
genome
nucleic acid
gene
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AU2017322733A1 (en
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John HUNZEKER
Matthew Johnson
Kanut LAOHARAWEE
Branden S. Moriarity
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University of Minnesota System
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University of Minnesota Twin Cities
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AU2017322733A 2016-09-12 2017-09-12 Genome edited primary B cell and methods of making and using Active AU2017322733B2 (en)

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US201662393512P 2016-09-12 2016-09-12
US62/393,512 2016-09-12
PCT/US2017/051182 WO2018049401A1 (en) 2016-09-12 2017-09-12 Genome edited primary b cell and methods of making and using

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AU2017322733A1 AU2017322733A1 (en) 2019-04-11
AU2017322733B2 true AU2017322733B2 (en) 2024-05-09

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US (1) US20220168342A1 (enExample)
EP (1) EP3509606A4 (enExample)
JP (2) JP2019526270A (enExample)
CN (1) CN109843303A (enExample)
AU (1) AU2017322733B2 (enExample)
CA (1) CA3036820A1 (enExample)
WO (1) WO2018049401A1 (enExample)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2018235957B2 (en) 2017-03-16 2024-02-01 Seattle Children's Hospital (dba Seattle Children's Research Institute) Engraftable cell-based immunotherapy for long-term delivery of therapeutic proteins
AU2020392222A1 (en) * 2019-11-27 2022-06-09 Board Of Regents, The University Of Texas System Large-scale combined CAR transduction and CRISPR gene editing of B cells
WO2023283585A2 (en) * 2021-07-06 2023-01-12 Vor Biopharma Inc. Inhibitor oligonucleotides and methods of use thereof
WO2023010125A1 (en) * 2021-07-29 2023-02-02 Regents Of The University Of Minnesota Multiplex base editing of primary human natural killer cells
EP4555091A2 (en) * 2022-07-13 2025-05-21 Vor Biopharma Inc. Compositions and methods for artificial protospacer adjacent motif (pam) generation
WO2024196669A2 (en) * 2023-03-17 2024-09-26 Walking Fish Therapeutics, Inc. Methods for in vivo editing of b cells

Citations (1)

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Publication number Priority date Publication date Assignee Title
WO2016100932A1 (en) * 2014-12-19 2016-06-23 Immusoft Corporation B cells for in vivo delivery of therapeutic agents

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US20170354681A1 (en) * 2014-10-24 2017-12-14 Bcrt Holding Bv T cell-based immunotherapeutics
EP4335918A3 (en) * 2015-04-03 2024-04-17 Dana-Farber Cancer Institute, Inc. Composition and methods of genome editing of b-cells

Patent Citations (1)

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Publication number Priority date Publication date Assignee Title
WO2016100932A1 (en) * 2014-12-19 2016-06-23 Immusoft Corporation B cells for in vivo delivery of therapeutic agents

Non-Patent Citations (2)

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Title
Herbig EJ, Hyland K, Xu M, de Laat R, Olson E, Aronovich E, Scholz M, Hackett P, McIvor RS. 373. Molecular Therapy. 2015 May 1;23:S148. (Year: 2015) *
TAEK-CHIN CHEONG ET AL: "Editing of mouse and human immunoglobulin genes by CRISPR-Cas9 system", NATURE COMMUNICATIONS, vol. 7, 9 March 2016 (2016-03-09), pages 10934, XP055272094, ISSN: 2041-1723, DOI: 10.1038/ncomms10934 *

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JP2019526270A (ja) 2019-09-19
WO2018049401A8 (en) 2019-04-04
US20220168342A1 (en) 2022-06-02
CA3036820A1 (en) 2018-03-15
EP3509606A1 (en) 2019-07-17
CN109843303A (zh) 2019-06-04
JP2022189863A (ja) 2022-12-22
EP3509606A4 (en) 2020-10-07
WO2018049401A1 (en) 2018-03-15
AU2017322733A1 (en) 2019-04-11

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